Mao Z S, Long Y J, Zhu Y Y, Zhu S S, He X H, Chen Z J
Key Laboratory of Plant Pathology of Yunnan Province, Yunnan Agricultural University, Kunming 650201, China.
Wenshan Sanqi Institute of Wenshan University, Wenshan 663000, and Wenshan Miaoxiang Notoginseng Industrial Co., Ltd, Wenshan 663000, China.
Plant Dis. 2014 Jan;98(1):162. doi: 10.1094/PDIS-11-12-1104-PDN.
Sanqi (Panax notoginseng (Burk.) F. H. Chen) is planted on >10,000 ha in China and is a popular Chinese medicinal material (2). Black root rot is a recently identified but worsening problem on Sanqi since 2010 in Wenshan, China. Of the plant tubers examined from 185 ha, 8.5 to 27.4% were black with necrotic lesions. The base of leaves of infected plants had brown, sunken, necrotic lesions, and symptomatic plants had one to three chlorotic leaves. A fungus was isolated consistently from the basal leaves, bulb, and tubers of symptomatic plants. Six single-spore isolates were cultured on potato sucrose agar (PSA) at 25 ± 1°C in the dark. The mycelium of each culture was white initially on PSA, and then became rust-colored. The adaxial surfaces of the plates were black. Conidiophores were 13.6 to 167.3 × 1.4 to 21.8 μm (avg. 68.6 × 2.9 μm), single or with up to four levels of branching and two to three branches (or phialides) per level. The basal branches were often divergent, whereas the terminal branches were usually more appressed. Sporodochia were not present. Microconidia were 0-septate, 4.1 to 9.5 × 2.7 to 4.1 μm (avg. 8.2 × 2.9 μm). Conidia were 1- to 3-septate and occasionally 4-septate. One- to 3-septate conidia were clavate, with a truncate or slightly protruding conidial base, 9.2 to 40.8 × 3.5 to 6.8 μm (avg. 26.7 × 5.2 μm); whereas 4-septate conidia were 32.6 to 50.3 × 5.4 to 6.8 μm (avg. 40.9 × 6.5 μm). Chlamydospores were abundant, golden to brown, single or in chains or clumps, and up to 21.8 μm in diameter. PCR amplification was carried out for one isolate, RR926, using rDNA internal transcribed spacer (ITS) primer pairs ITS1F and ITS4 (4). Sequencing of the PCR product (GenBank Accession No. KC904953) revealed 99% similarity (99% coverage) with the ITS sequence of Cylindrocarpon destructans var. destructans (AM419065). Phylogenetic analysis (MEGA 4.1) using the neighbor-joining algorithm placed the isolate in a well-supported cluster (>90% bootstrap value based on 1,000 replicates) with AM419065. Therefore, the pathogen was identified as C. destructans (Zinssm.) Scholten var. destructans (teleomorph Ilyonectria radicicola (Gerlach & L. Nilsson) P. Chaverri & C. Salgado) based on morphological characteristics and rDNA-ITS sequence analysis (1,3). Pathogenicity tests of the six isolates were conducted on five 1-year-old and five 3-year-old plants/isolate. The roots of all plants were washed with sterilized water, and then surface-sterilized with 75% ethanol. Inoculum (1 ml of 10 conidia/ml) of each isolate was brushed onto the roots of each plant with a paintbrush. Inoculated plants were planted in pots in a mixture of sterilized quartz sand:vermiculite:pearlite (2:1:1, v/v). The pots were placed under black shadecloth. The roots of five 1-year-old and five 3-year-old plants were brushed similarly with sterilized water as control treatments. After 30 days, symptoms similar to those on the original diseased plants were observed on the roots of all plants inoculated with the six isolates. The roots of non-inoculated plants remained healthy. The experiment was repeated. The same pathogen was re-isolated from the inoculated plants, but no pathogen was isolated from roots of the control plants. C. destructans var. destructans is widely distributed in soils (1), but to our knowledge, this is the first report of this fungus causing black root rot of Sanqi in China. References: (1) P. Charerri et al. Stud. Mycol. 68:57, 2011. (2) C. Y. Hu. New Rural Technol. 2:59, 2013 (in Chinese). (3) K. A. Seifert and P. E. Axelrood. Can. J. Plant Pathol. 20:115, 1998. (4) K. A. Seifert et al. Phytopathology 93:1533, 2003.
三七(Panax notoginseng (Burk.) F. H. Chen)在中国的种植面积超过10000公顷,是一种广受欢迎的中药材(2)。黑根腐病是近年来在中国文山地区三七上发现的一个日益严重的问题。在检查的185公顷种植块茎中,8.5%至27.4%的块茎呈现黑色并带有坏死斑。受感染植株的叶基部有褐色、凹陷的坏死斑,发病植株有1至3片黄化叶。从发病植株的基部叶片、鳞茎和块茎中 consistently 分离出一种真菌。将6个单孢分离株在马铃薯蔗糖琼脂(PSA)上于25±1°C黑暗条件下培养。每种培养物的菌丝体最初在PSA上为白色,然后变为锈色。平板的正面为黑色。分生孢子梗长13.6至167.3×1.4至21.8μm(平均68.6×2.9μm),单生或有多达四级分支,每级有2至3个分支(或瓶梗)。基部分支通常向外伸展,而末端分支通常更贴伏。无分生孢子座。小型分生孢子无隔膜,4.1至9.5×2.7至4.1μm(平均8.2×2.9μm)。分生孢子有1至3个隔膜,偶尔有4个隔膜。1至3个隔膜的分生孢子呈棒状,分生孢子基部截形或稍突出,9.2至40.8×3.5至6.8μm(平均26.7×5.2μm);而4个隔膜的分生孢子为32.6至50.3×5.4至6.8μm(平均40.9×6.5μm)。厚垣孢子丰富,金黄色至褐色,单生或成链状或团块状,直径可达21.8μm。对一个分离株RR926使用rDNA内转录间隔区(ITS)引物对ITS1F和ITS4进行PCR扩增(4)。PCR产物测序(GenBank登录号KC904953)显示与毁灭柱孢变种毁灭柱孢(AM419065)的ITS序列有99%的相似性(99%的覆盖率)。使用邻接法(MEGA 4.1)进行系统发育分析,将该分离株置于一个支持度良好的聚类中(基于1000次重复的自展值>90%),与AM419065聚在一起。因此,根据形态特征和rDNA-ITS序列分析(1,3),该病原菌被鉴定为毁灭柱孢(Zinssm.)Scholten变种毁灭柱孢(有性型为放射状伊氏霉(Gerlach & L. Nilsson)P. Chaverri & C. Salgado)。对这6个分离株对5株1年生和5株3年生植株进行致病性测试。所有植株的根先用无菌水冲洗,然后用75%乙醇进行表面消毒。用画笔将每个分离株的接种物(1ml含10个分生孢子/ml)刷到每株植物的根上。接种后的植株种植在装有灭菌石英砂:蛭石:珍珠岩(2:1:1,v/v)混合物的花盆中。花盆置于黑色遮阳网下。对5株1年生和5株3年生植株的根同样用无菌水刷洗作为对照处理。30天后,在接种了这6个分离株的所有植株的根上观察到与原始患病植株相似的症状。未接种植株的根保持健康。该实验重复进行。从接种植株中再次分离到相同病原菌,但从对照植株的根中未分离到病原菌。毁灭柱孢变种毁灭柱孢在土壤中广泛分布(1),但据我们所知,这是该真菌在中国引起三七黑根腐病的首次报道。参考文献:(1)P. Charerri等人,《Stud. Mycol.》68:57,2011。(2)C. Y. Hu,《新农村技术》2:59,2013(中文)。(3)K. A. Seifert和P. E. Axelrood,《加拿大植物病理学杂志》20:115,1998。(4)K. A. Seifert等人,《植物病理学》93:1533,2003。